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Safety and Bacteraemia Between Peripherally Inserted and Central Inserted Catheters. (PYCBAC)

F

Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Status

Completed

Conditions

Catheter Related Infections

Treatments

Device: CVC
Device: PICC

Study type

Interventional

Funder types

Other

Identifiers

NCT02538159
IIBSP-CAT-2014-36

Details and patient eligibility

About

Clinical, prospective, single-center, national trial. open and randomized at 1: 1 to compare the rate of bacteremia associated between non-tunneled Central venous catheter and peripheral inserted central catheter.

Enrollment

247 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male and female patients ≥ 18 years.
  • Patients hospitalized at our institution requiring at least 6 days of intravenous treatment in a conventional ward of our hospital.
  • Signed informed consent by the patient and / or when necessary parent / legal guardian.

Exclusion criteria

  • Patients with bacteremia at the time of catheter insertion.
  • Patients admitted to hematology or intensive care units, for considered a type of patient characteristics very different from other patients.
  • Patients with severe clinical situation.
  • Patients in whom peripheral venous access is technically impossible, patients outpatient and express refusal of the patient.
  • Pregnant patients.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

247 participants in 2 patient groups

Experimental CVC
Experimental group
Description:
CVC insertion Non-tunneled Central venous catheter insertion
Treatment:
Device: CVC
Experimental PICC
Experimental group
Description:
PICC insertion Peripherally inserted catheter
Treatment:
Device: PICC

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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